Distinct enzyme combinations in AKAP signalling complexes permit functional diversity
- 16 October 2005
- journal article
- research article
- Published by Springer Nature in Nature Cell Biology
- Vol. 7 (11) , 1066-1073
- https://doi.org/10.1038/ncb1315
Abstract
Specificity in cell signalling can be influenced by the targeting of different enzyme combinations to substrates. The A-kinase anchoring protein AKAP79/150 is a multivalent scaffolding protein that coordinates the subcellular localization of second-messenger-regulated enzymes, such as protein kinase A, protein kinase C and protein phosphatase 2B. We developed a new strategy that combines RNA interference of the endogenous protein with a protocol that selects cells that have been rescued with AKAP79/150 forms that are unable to anchor selected enzymes. Using this approach, we show that AKAP79/150 coordinates different enzyme combinations to modulate the activity of two distinct neuronal ion channels: AMPA-type glutamate receptors and M-type potassium channels. Utilization of distinct enzyme combinations in this manner provides a means to expand the repertoire of cellular events that the same AKAP modulates.Keywords
This publication has 31 references indexed in Scilit:
- AKAP150 signaling complex promotes suppression of the M-current by muscarinic agonistsNature Neuroscience, 2003
- Assembly of Cell Regulatory Systems Through Protein Interaction DomainsScience, 2003
- PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticityNature Neuroscience, 2003
- Mapping the Protein Phosphatase-2B Anchoring Site on AKAP79Published by Elsevier ,2002
- Recovery from Muscarinic Modulation of M Current Channels Requires Phosphatidylinositol 4,5-Bisphosphate SynthesisNeuron, 2002
- The Sequence of the Human GenomeScience, 2001
- Initial sequencing and analysis of the human genomeNature, 2001
- Signaling—2000 and BeyondCell, 2000
- Modulation of Ion Channels: A “Current” View of AKAPsNeuron, 1999
- Regulation of NMDA Receptors by an Associated Phosphatase-Kinase Signaling ComplexScience, 1999